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Volumn 33, Issue 7, 1994, Pages 728-729

Resolution of Racemates by Distillation with Inclusion Compounds

Author keywords

[No Author keywords available]

Indexed keywords


EID: 33748224273     PISSN: 05700833     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.199407281     Document Type: Article
Times cited : (59)

References (28)
  • 8
    • 0001004673 scopus 로고
    • (R)- und (S)-4-Alkoxy-2-tert-butyl-2,5-dihydroimidazol-1-carbonsäureester – neue chirale Glycinderivate für die Aminosäuresynthese
    • Recent example
    • (1993) Angewandte Chemie , vol.105 , pp. 1780
    • Blank, S.1    Seebach, D.2
  • 11
    • 0002484863 scopus 로고
    • Isolation and optical resolution of materials utilizing inclusion crystallization
    • (1987) Top. Curr. Chem. , vol.140 , pp. 43
    • Toda, F.1
  • 12
    • 0000741239 scopus 로고
    • J. L. Atwood, J. E. D. Davies, D. D. MacNicol, Oxford University Press, Oxford
    • (1991) Inclusion Compounds , vol.4 , pp. 126
    • Toda, F.1
  • 15
    • 84989521616 scopus 로고    scopus 로고
    • Of course this is not true for the diastereoselective reactions of chiral natural products, for example, steroids.
  • 17
    • 0011154326 scopus 로고
    • Trennung der Enantiomere von 2,2′-Dihydroxy-1,1′-binaphthyl und 10,10′-Dihydroxy-9,9′-biphenanthryl durch Komplexierung mitN-Alkyl-cinchonidiniumhalogeniden
    • (1993) Angewandte Chemie , vol.105 , pp. 1266
    • Tanaka, K.1    Okada, T.2    Toda, F.3
  • 25
    • 84989593468 scopus 로고    scopus 로고
    • The molecule in ref.[9] (there 1a,b,c) is shown with the (S,S)configuration but labeled “(R,R)”. Upon Subsequent inquiry the correspondence author replied that “(R,R)‐(–)” is correct. The optical rotations in the table apply to this configuration.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.